Symbol Name ID |
Slc39a4
solute carrier family 39 (zinc transporter), member 4 MGI:1919277 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Hepatomegaly |
Short stature |
Failure to thrive |
Disease(s) Associated with SLC39A4 | ||||
acrodermatitis enteropathica |
Mouse Phenotypes | embryonic growth retardation |
decreased embryo size |
weight loss |
abnormal head morphology |
decreased body size |
postnatal growth retardation |
|
Availability | Mouse Genotype | ||||||
Slc39a4tm1Gka/Slc39a4+ | |||||||
Slc39a4tm2Gka/Slc39a4tm2Gka Tg(Vil1-cre/ERT2)23Syr/0 (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/02/2024 MGI 6.24 |
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